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P Rinaldo

Showing results (81-90 of 95) with videos related to

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Cytokine|January 6, 2022
Role of immune mediators in predicting hospitalization of SARS-CoV-2 positive patientsS Ashrafzadeh-Kian, M R Campbell, J C Jara Aguirre, et al.
Molecular Genetics and Metabolism|March 24, 2010
Maple syrup urine disease: further evidence that newborn screening may fail to identify variant formsR L Puckett, F Lorey, P Rinaldo, et al.
The American Journal of Gastroenterology|November 1, 1996
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, M E Shoup, D E Hale, et al.
Clinical Chemistry|February 5, 2000
Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidationP M Jones, R Quinn, P V Fennessey, et al.
Human Molecular Genetics|October 9, 2001
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouseK B Cox, D A Hamm, D S Millington, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Therapeutic trial in the first three Asian cases of ethylmalonic encephalopathy: response to riboflavinH R Yoon, S H Hahn, Y M Ahn, et al.
The Journal of Pediatrics|June 17, 1998
Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of lifeR G Boles, E A Buck, M G Blitzer, et al.
The American Journal of Physiology|May 1, 1996
Noninvasive probing of citric acid cycle intermediates in primate liver with phenylacetylglutamineD Yang, S F Previs, C A Fernandez, et al.
Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidationD M Kurtz, P Rinaldo, W J Rhead, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Cytokine|January 6, 2022
Role of immune mediators in predicting hospitalization of SARS-CoV-2 positive patientsS Ashrafzadeh-Kian, M R Campbell, J C Jara Aguirre, et al.
Molecular Genetics and Metabolism|March 24, 2010
Maple syrup urine disease: further evidence that newborn screening may fail to identify variant formsR L Puckett, F Lorey, P Rinaldo, et al.
The American Journal of Gastroenterology|November 1, 1996
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, M E Shoup, D E Hale, et al.
Clinical Chemistry|February 5, 2000
Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidationP M Jones, R Quinn, P V Fennessey, et al.
Human Molecular Genetics|October 9, 2001
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouseK B Cox, D A Hamm, D S Millington, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Therapeutic trial in the first three Asian cases of ethylmalonic encephalopathy: response to riboflavinH R Yoon, S H Hahn, Y M Ahn, et al.
The Journal of Pediatrics|June 17, 1998
Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of lifeR G Boles, E A Buck, M G Blitzer, et al.
The American Journal of Physiology|May 1, 1996
Noninvasive probing of citric acid cycle intermediates in primate liver with phenylacetylglutamineD Yang, S F Previs, C A Fernandez, et al.
Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidationD M Kurtz, P Rinaldo, W J Rhead, et al.
Pageof 10